| Tag | Content |
|---|
EnhancerAtlas ID | HS060-00278 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr1:11024950-11026410 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:11025700-11025715 | GAGGTCAGAAGCTCA | + | 6.15 | | RARA | MA0729.1 | chr1:11025700-11025718 | GAGGTCAGAAGCTCAAGA | + | 6.01 | | SPIB | MA0081.2 | chr1:11025389-11025401 | AAAGGGGAAGTG | + | 6.07 | | ZNF263 | MA0528.1 | chr1:11025271-11025292 | AGAGGAAGAGAAAGAGGAGGA | + | 7.36 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I010964 | chr1 | 11024590 | 11026962 |
|
Enhancer Sequence | GTGCTGGGAT TACAGGCGTG AGCCACCAAG CCCAGCCAAG GCTGGGTTTA TGAGACATAA 60
AATTCCCATT TTACAGATGA GGCAGTTGAG GCTTAGAGAA GGTAAATGAC TAAGCCAAAG 120
GCATGTGGCC ATTTCTGAGA CTAGATGTGA GAGCTGGTCT AGCTCATTCC GGTACAAGGC 180
GGACTTCAAA GATGTCAAAC CAATGGGTCC CTCTGCCCCT CCCAGGCTGC CCTCATTCAG 240
CCACATAAGA AGAACCCAAG TCTAAGCTTT GCGGTGGGGC CTGAGAAGGG TGACGGGGCT 300
GTCAGAGAAG GGCGACCACA GAGAGGAAGA GAAAGAGGAG GAGCAGGGTA GTTCCCAAAA 360
TTCCTTCCCC CACTCCAGAC CACAGCCCCA CTCAGGAAAA ACTCTGGACT GGGTCAAGGA 420
AGGGAGCACA AAGAAATGGA AAGGGGAAGT GGAGGTGAGG AAAAGACAAG AAAAAAAAAA 480
CTGTGAGCCA AACTGTGCGG CTGGTTGTCC CCTTGCAGGA CCCCTGGAGT GAAATTTAAG 540
TAACAAGAAT GCTGGCACAG TGGCTCATTC CTATCATCTC AACACATTGG GACACCGAGG 600
CGGGAGGATG GCTTGAGCCT GGGAATTCCA GACCAGCCTG GGCAACATGG TGAAACCCCA 660
TCTTCTACAA AAAGTACAAA AATTACCTGG GTGTAGTGGT GCATGCCTGT AGTCCCAGCT 720
ACTCTGGGGG CCGAGGTGGG TGGATCACTT GAGGTCAGAA GCTCAAGACC AGCCTGGCCA 780
ACAAGGTGAA ACCCCGCCTT TACCAAGTAG TCTCAGCTAC TTCAGAGGCT GAGGCAGGGG 840
AATCGCTTGA ACCTGGGAGG CGGAAGTTGC AGTGAGCCGA GATTGCGTCA CTGCACTCCA 900
GCCTGGGTGC CAGAGCGAGC CTCCGTCAAA AAAAAAAAAA AAAGGAAAAA GAATACAAAA 960
ATATCTTGCT TCTGTAAATT TTAGAGTCAC ATGGTCTCGT GAGCCCATAA TGGGCCTGTG 1020
CAAGTGAGGG CTGTCAGTCA GTCTTTGCAA CTCCTCAGCA CCATTTATTC ACTTCATTCA 1080
GCACTTACTG AGTACCTACT GTGTGCCAGG CCCTGAGGCA AGCCTGTGGG TGTGACTGCC 1140
TCACCCCAGA GACTCCAGGT CCAGCAGGAT ATGGTGTGTG AGTGGGCACA TTATGAGTCA 1200
GTGTTGGCAA TGATAGAAGC AGGTCTACTG CACAGAGAAG GGGGGATTCT CAGGAGGACT 1260
GCCTGGAGGA GGCAGCATCT GAGCTGGGCG GCCTTTTAAT ATCTATGCCC ATAAACTCCA 1320
TGAGGGCAGA GACTTCTGGT CTCCCTCAGC TCAGTTTCTG CAGAGGAATA ATGGTGCAGT 1380
GTCTCCTTAC TTGATATCTG AGCTCAGGCT TAGCTCCTTA AATCTCCCTT TAAAAAAAAA 1440
AAAAGAAAAG TTTCCCAAAC 1460
|
